Allele Registry

Canonical Allele Identifier: PA104739

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV000011657

ClinVar Variation:

10910

HGVS (amino-acid)	Matching Registered Transcripts
NP_002342.1:p.Arg55Leu	CA255607 NM_002351.5:c.164G>T